Cas 1208251-51-7,4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid

1208251-51-7

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Basic information

Product Name: 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid
Synonyms: 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid
CAS NO:1208251-51-7
Molecular Formula:
Molecular Weight: 336.434
EINECS: N/A
Product Categories: N/A
Mol File: 1208251-51-7.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid(CAS DataBase Reference)
NIST Chemistry Reference: 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid(1208251-51-7)
EPA Substance Registry System: 4-{5-[2-(2,6,6-trimethylcyclohex-2-en-1-yl)ethenyl]-1H-pyrazol-1-yl}benzoic acid(1208251-51-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1208251-51-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1208251-51-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,8,2,5 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1208251-51:
(9*1)+(8*2)+(7*0)+(6*8)+(5*2)+(4*5)+(3*1)+(2*5)+(1*1)=117
117 % 10 = 7
So 1208251-51-7 is a valid CAS Registry Number.

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1208251-51-7Relevant articles and documents

Antiproliferative and proapoptotic activities of a new class of pyrazole derivatives in HL-60 cells

Anzaldi, Maria,Maccio, Chiara,Mazzei, Mauro,Bertolotto, Maria,Ottonello, Luciano,Dallegri, Franco,Balbi, Alessandro

experimental part, p. 1674 - 1687 (2010/05/18)

A series of N-substituted pyrazole derivatives have been synthesized and tested for their anticancer effect on the HL-60 leukaemia cell line. Four were active both in cell-growth inhibition and in inducing apoptosis. The inhibition of cell growth mainly r

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